Acrorenal field (Development)Bardet Biedl syndromeC1r (Complement)C1s (Complement)C2 (Complement)C3 (Complement)C4 (Complement)C5 (Complement)C6 (Complement)C7 (Complement)C8 (Complement)C9 (Complement)Caudal regression syndromeCloaca (Exstrophy)EBV Epstein barr virus
Factor B (Complement)Factor I (Complement)Familial hyperuricemic nephropathyFetal Warfarin SyndromeHand and Wrist (Malformation)Hereditary renal hypouricemiaHydrolethalus SyndromeHypergammaglobulinemia idiopathicHyperglobulinemic purpuraIgM NephropathyIvemark s syndromeKidney (Agenesis)Kidney (C3NEF)Kidney (Intercalated cell)Kidney (Macula densa)
Kidney (Medullary cystic disease)Kidney (Medullary sponge kidney)Kidney (Podocytes)Kidney (Principal cells)Kidney (Radiation nephritis)Kidney (REPOS cells)Kidney (Tip lesion)Kidney (Toxicology)Kidney (Tubulus MCD)Magnesium (Physiology Intestines)Muckle Wells syndromeNephrinPallister Hall SyndromePCD (Heavy chain disease)PKHD1
Poland s anomalyPolytopic acrorenal developmental field defectPotter s sequenceRadius (Aplasia)Robinson s defectSLC22A12 URAT1SyndactylyTTC8Urinary blader (Megacystis)Urinary tract (Obstructive uropathy)Varicella zoster viruszztrash
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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.